Indian Hedgehog Regulates Intestinal Stem Cell Fate Through Epithelial-Mesenchymal Interactions During Development

被引:92
|
作者
Kosinski, Cynthia [3 ]
Stange, Daniel E. [4 ,5 ]
Xu, Chuanrui [3 ]
Chan, Annie Sy [1 ,2 ]
Ho, Coral [3 ]
Yuen, Siu Tsan [1 ,2 ]
Mifflin, Randy C. [6 ]
Powell, Don W. [6 ]
Clevers, Hans [4 ,5 ]
Leung, Suet Yi [1 ,2 ]
Chen, Xin [3 ]
机构
[1] Univ Hong Kong, Queen Mary Hosp, Dept Pathol, Pokfulam, Hong Kong, Peoples R China
[2] Univ Hong Kong, Queen Mary Hosp, Ctr Canc Res, Pokfulam, Hong Kong, Peoples R China
[3] Univ Calif San Francisco, Dept Bioengn & Therapeut Sci, San Francisco, CA 94143 USA
[4] Univ Med Ctr Utrecht, Utrecht, Netherlands
[5] KNAW, Hubrecht Inst, Utrecht, Netherlands
[6] Univ Texas Galveston, Med Branch, Dept Internal Med, Galveston, TX 77550 USA
基金
美国国家卫生研究院;
关键词
Hedgehog Signaling; ECM; MMP; BMP; COLORECTAL-CANCER CELLS; SIGNALING PATHWAY; SELF-RENEWAL; BETA-CATENIN; CRYPT; DIFFERENTIATION; EXPRESSION; TRANSCRIPTION; REQUIREMENT; HOMEOSTASIS;
D O I
10.1053/j.gastro.2010.06.014
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
BACKGROUND & AIMS: Intestinal stem cells (ISCs) are regulated by the mesenchymal environment via physical interaction and diffusible factors. We examined the role of Indian hedgehog (Ihh) in mesenchymal organization and the mechanisms by which perturbations in epithelial-mesenchymal interactions affect ISC fate. METHODS: We generated mice with intestinal epithelial-specific disruption of Ihh. Gross and microscopic anatomical changes were determined using histologic, immunohistochemical, and in situ hybridization analyses. Molecular mechanisms were elucidated by expression profiling and in vitro analyses. RESULTS: Deletion of intestinal epithelial Ihh disrupted the intestinal mesenchymal architecture, demonstrated by loss of the muscularis mucosae, deterioration of the extracellular matrix, and reductions in numbers of crypt myofibroblasts. Concurrently, the epithelial compartment had increased Wnt signaling, disturbed crypt polarity and architecture, defective enterocyte differentiation, and increased and ectopic proliferation that was accompanied by increased numbers of ISCs. Mechanistic studies revealed that Hh inhibition deregulates bone morphogenetic protein signaling, increases matrix metalloproteinase levels, and disrupts extracellular matrix proteins, fostering a proliferative environment for ISCs and progenitor cells. CONCLUSIONS: Ihh regulates ISC self-renewal and differentiation. Intestinal epithelial Ihh signals to the mesenchymal compartment to regulate formation and proliferation of mesenchymal cells, which in turn affect epithelial proliferation and differentiation. These findings provide a basis for analyses of the role of the muscularis mucosae in ISC regulation.
引用
收藏
页码:893 / 903
页数:11
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